AR017217A1 - BISPIDINE ANTIARRITHMIC COMPOUNDS, PHARMACEUTICAL FORMULATION, USE OF THE SAME TO PREPARE MEDICINES, PROCESS TO PREPARE SUCH COMPOUNDS, INTERMEDIARY COMPOUNDS, AND PROCESS TO PREPARE THEM - Google Patents

BISPIDINE ANTIARRITHMIC COMPOUNDS, PHARMACEUTICAL FORMULATION, USE OF THE SAME TO PREPARE MEDICINES, PROCESS TO PREPARE SUCH COMPOUNDS, INTERMEDIARY COMPOUNDS, AND PROCESS TO PREPARE THEM

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Publication number
AR017217A1
AR017217A1 ARP980106399A ARP980106399A AR017217A1 AR 017217 A1 AR017217 A1 AR 017217A1 AR P980106399 A ARP980106399 A AR P980106399A AR P980106399 A ARP980106399 A AR P980106399A AR 017217 A1 AR017217 A1 AR 017217A1
Authority
AR
Argentina
Prior art keywords
prepare
compounds
alkyl
group
independently represent
Prior art date
Application number
ARP980106399A
Other languages
Spanish (es)
Original Assignee
Astrazeneca Ab
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Astrazeneca Ab filed Critical Astrazeneca Ab
Publication of AR017217A1 publication Critical patent/AR017217A1/en

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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/08Bridged systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/06Antiarrhythmics

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  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Cardiology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

Un compuesto que comprende la formula(I) en la cual R1 y R2 independientemente representan H, alquilo C1-4 o juntos forman -O-(CH2)2-O-, -(CH2)4 -o-(CH2)5R9 representa alquilo C1-12, fenilo, naftilo, alquilfenilo C1-3 (estando todos estos cuatro grupos optativamente sustituidos o terminados con uno o mássustituyentes seleccionados entre -OH, halo, ciano,nitro, alquilo C1-4 o alcoxi C1-4) o-(CH2)qCy1; R10 representa H o -OH; R11 representa H o alquilo C1-4, R12representa uno o más sustituyentes optativos seleccionados entre -OH, ciano, halo, amino, nitro, alquilo C1-6, alcoxi C1-6, -N(H)S(O)2R16, -OS(O)2R16a,N(H)C(O)N(H)R17 o -C(O)N(H)R18; A representaun enlace simple, alquileno C1-4, -(CH2)nN(R20), -(CH2)nS(O)p- -(CH2)NO- (estando elgrupo -(CH2)n- de estos tres ultimos grupos unido al átomo de carbono que contiene R10 y R11), -C(O)N(R20)- (estando el grupo -C(O) de éste ultimo grupo unidoal átomo de carbono que contiene R10 y R11), -N(R20)C(O)O(CH2)n-, -N(R20)(CH2)n- (en estos dos ultimos grupos, el grupo N(R20) está unido al átomo de carbonoque acarrea R10 y R11) o -(CH2)mC(H)(OH)(CH2)n- (es este ultimo grupo, el grupo -(CH2)m- está unido al átomo de carbono que acarrea R10 y R11); B representa unenlace simple, alquileno C1-6, -N(R23)(CH2)r - o -O(CH2)r (en estos dos ultimos grupos, el grupo -(CH2)r está unido al átomo de nitrogeno de la bispidina); mrepresenta 1, 2 o 3; n y r representan independientemente 0,1,2,3 o 4; p representa 0,1 o 2; q representa 0,1,2 o 3; X representa O o S; Cy1 representa unanillo heterocíclico de cinco a siete miembros que contiene uno o más heteroátomos seleccionados entre O, N o S, anillo que está optativamente sustituido conuno o más sustituyentes seleccionados entre C(O)R21 o C(O)OR22, R16, R16a, R20 y R23 representan independientemente H o alquilo C1-4 y R17, R18, R21 y R22representan independientemente H o alquilo C1-4 y R17, R18, R21 y R22 representan independientemente H o alquilo C1-6; o un derivado farmacéuticamenteA compound comprising the formula (I) in which R1 and R2 independently represent H, C1-4 alkyl or together form -O- (CH2) 2-O-, - (CH2) 4 -o- (CH2) 5R9 represents C1-12 alkyl, phenyl, naphthyl, C1-3 alkylphenyl (all four groups being optionally substituted or terminated with one or more substituents selected from -OH, halo, cyano, nitro, C1-4 alkyl or C1-4 alkoxy) or- (CH2) qCy1; R10 represents H or -OH; R11 represents H or C1-4 alkyl, R12 represents one or more optional substituents selected from -OH, cyano, halo, amino, nitro, C1-6 alkyl, C1-6 alkoxy, -N (H) S (O) 2R16, - OS (O) 2R16a, N (H) C (O) N (H) R17 or -C (O) N (H) R18; A represents a single bond, C1-4 alkylene, - (CH2) nN (R20), - (CH2) nS (O) p- - (CH2) NO- (the group being - (CH2) n- of these last three groups attached to the carbon atom containing R10 and R11), -C (O) N (R20) - (the group -C (O) of the latter being attached to the carbon atom containing R10 and R11), -N (R20) C (O) O (CH2) n-, -N (R20) (CH2) n- (in these last two groups, the group N (R20) is attached to the carbon atom that carries R10 and R11) or - (CH2) mC (H) (OH) (CH2) n- (is the latter group, the group - (CH2) m- is attached to the carbon atom that carries R10 and R11); B represents a simple bond, C1-6 alkylene, -N (R23) (CH2) r - or -O (CH2) r (in these last two groups, the group - (CH2) r is attached to the bispidine nitrogen atom ); mrepresenta 1, 2 or 3; n and r independently represent 0,1,2,3 or 4; p represents 0.1 or 2; q represents 0,1,2 or 3; X represents O or S; Cy1 represents a five to seven membered heterocyclic ring containing one or more heteroatoms selected from O, N or S, ring that is optionally substituted with one or more substituents selected from C (O) R21 or C (O) OR22, R16, R16a, R20 and R23 independently represent H or C1-4 alkyl and R17, R18, R21 and R22 independently represent H or C1-4 alkyl and R17, R18, R21 and R22 independently represent H or C1-6 alkyl; or a pharmaceutically derived

ARP980106399A 1997-12-17 1998-12-16 BISPIDINE ANTIARRITHMIC COMPOUNDS, PHARMACEUTICAL FORMULATION, USE OF THE SAME TO PREPARE MEDICINES, PROCESS TO PREPARE SUCH COMPOUNDS, INTERMEDIARY COMPOUNDS, AND PROCESS TO PREPARE THEM AR017217A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
SE9704709A SE9704709D0 (en) 1997-12-17 1997-12-17 Pharmaceutically active compounds

Publications (1)

Publication Number Publication Date
AR017217A1 true AR017217A1 (en) 2001-08-22

Family

ID=20409426

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP980106399A AR017217A1 (en) 1997-12-17 1998-12-16 BISPIDINE ANTIARRITHMIC COMPOUNDS, PHARMACEUTICAL FORMULATION, USE OF THE SAME TO PREPARE MEDICINES, PROCESS TO PREPARE SUCH COMPOUNDS, INTERMEDIARY COMPOUNDS, AND PROCESS TO PREPARE THEM

Country Status (28)

Country Link
US (1) US6291475B1 (en)
EP (1) EP1047695B1 (en)
JP (1) JP2002508375A (en)
KR (1) KR20010024723A (en)
CN (1) CN1284956A (en)
AR (1) AR017217A1 (en)
AT (1) ATE261964T1 (en)
AU (1) AU1795399A (en)
BR (1) BR9813668A (en)
CA (1) CA2314490A1 (en)
DE (1) DE69822513T2 (en)
DK (1) DK1047695T3 (en)
EE (1) EE200000365A (en)
ES (1) ES2216337T3 (en)
HU (1) HUP0102307A3 (en)
ID (1) ID24638A (en)
IL (1) IL136374A0 (en)
IS (1) IS5522A (en)
NO (1) NO20003137L (en)
NZ (1) NZ504909A (en)
PL (1) PL341388A1 (en)
PT (1) PT1047695E (en)
SE (1) SE9704709D0 (en)
SI (1) SI1047695T1 (en)
SK (1) SK7812000A3 (en)
TR (1) TR200001757T2 (en)
WO (1) WO1999031100A1 (en)
ZA (1) ZA9811130B (en)

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SE9803517D0 (en) * 1998-10-15 1998-10-15 Astra Ab Pharmaceutical preparation
TWI229674B (en) 1998-12-04 2005-03-21 Astra Pharma Prod Novel triazolo[4,5-d]pyrimidine compounds, pharmaceutical composition containing the same, their process for preparation and uses
SE9902269D0 (en) * 1999-06-16 1999-06-16 Astra Ab Pharmaceutically active compounds
SE9902270D0 (en) 1999-06-16 1999-06-16 Astra Ab Pharmaceutically active compounds
SE9902271D0 (en) * 1999-06-16 1999-06-16 Astra Ab Pharmaceutically active compounds
US20050004113A1 (en) * 1999-06-16 2005-01-06 Astrazeneca Ab New bispidine compounds useful in the treatment of cardiac arrhythmias
US20040229900A1 (en) * 1999-06-16 2004-11-18 Astrazeneca Ab Bispidine compounds useful in the treatment of cardiac arrythmias
SE9902268D0 (en) * 1999-06-16 1999-06-16 Astra Ab Pharmaceutically active compounds
US7038054B1 (en) * 1999-09-03 2006-05-02 Pharmacopeia Drug Discovery, Inc. Diazabicyclononane scaffold for combinatorial synthesis
SE9903759D0 (en) * 1999-10-18 1999-10-18 Astra Ab Pharmaceutically active compounds
JP2003516988A (en) 1999-12-14 2003-05-20 ニューロサーチ、アクティーゼルスカブ New heteroaryl-diazabicycloalkanes
SE9904765D0 (en) 1999-12-23 1999-12-23 Astra Ab Pharmaceutically useful compounds
AR030302A1 (en) * 2000-07-07 2003-08-20 Astrazeneca Ab BISPIDINE COMPOUNDS, PHARMACEUTICAL FORMULATION, USE FOR THE MANUFACTURE OF MEDICINES, PROCESS FOR THE PREPARATION OF THESE INTERMEDIATE COMPOUNDS AND COMPOUNDS
SE0002603D0 (en) * 2000-07-07 2000-07-07 Astrazeneca Ab New compounds
US6808924B1 (en) 2000-07-11 2004-10-26 Claudia Lanari Mouse mammary tumor lines expressing estrogen and progesterone receptors
AR030756A1 (en) 2000-10-02 2003-09-03 Astrazeneca Ab COMPOUND OF OXABISPIDINE USEFUL IN THE TREATMENT OF CARDIAC ARRITMIES
SE0003795D0 (en) 2000-10-20 2000-10-20 Astrazeneca Ab Pharmaceutically useful compounds
SE0100326D0 (en) 2001-02-02 2001-02-02 Astrazeneca Ab New compounds
SE0101329D0 (en) * 2001-04-12 2001-04-12 Astrazeneca Ab Pharmaceutical formulation
SE0101324D0 (en) * 2001-04-12 2001-04-12 Astrazeneca Ab New process
SE0101327D0 (en) * 2001-04-12 2001-04-12 Astrazeneca Ab New crystalline forms
TWI259836B (en) * 2001-04-12 2006-08-11 Astrazeneca Ab Modified release formulation suitable for antiarrhythmic compounds
JP2004538268A (en) * 2001-06-01 2004-12-24 ニューロサーチ、アクティーゼルスカブ Novel heteroaryl-diazabicycloalkanes as CNS-modulators
TW200418468A (en) * 2002-11-18 2004-10-01 Solvay Pharm Gmbh Liquid pharmaceutical formulations containing 3,7-diazabicyclo[3,3,1]nonane compounds and method of treatments relating to anti-arrhytmic events
EP1730145A1 (en) * 2004-03-22 2006-12-13 Boehringer Ingelheim Pharmaceuticals Inc. Alpha-trifluoromethyl alcohols or amines as glucocorticoid mimetics
SE0401539D0 (en) 2004-06-15 2004-06-15 Astrazeneca Ab New compounds
SE0401540D0 (en) 2004-06-15 2004-06-15 Astrazeneca Ab New compounds
WO2006135316A1 (en) 2005-06-13 2006-12-21 Astrazeneca Ab New oxabispidine compounds for the treatment of cardiac arrhythmias
CN102485725B (en) * 2010-12-02 2015-07-22 武汉药明康德新药开发有限公司 Diazacyclo bridged medicine template, preparation method thereof and application thereof
WO2012172043A1 (en) 2011-06-15 2012-12-20 Laboratoire Biodim Purine derivatives and their use as pharmaceuticals for prevention or treatment of bacterial infections
CN102875550B (en) * 2011-07-12 2016-01-06 常州合全药业有限公司 1,3,7-tri-replaces-3,7-diazabicyclos [3,3,1] nonane derivatives and preparation method
CN104151277A (en) * 2014-06-30 2014-11-19 北京万全德众医药生物技术有限公司 Preparation method of oxidation impurity dronedarone hydrochloride
CN113683585B (en) * 2021-09-26 2023-07-11 齐鲁工业大学 Preparation method of epoxy group-containing phthalonitrile monomer

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DE2428792A1 (en) 1974-06-14 1976-01-02 Knoll Ag NEW ANTIARRHYTHMICS
DE3112055A1 (en) 1981-03-27 1982-10-07 Basf Ag, 6700 Ludwigshafen BISPIDINE DERIVATIVES, THEIR PRODUCTION AND THE MEDICINAL PRODUCTS CONTAINING THEM
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Also Published As

Publication number Publication date
KR20010024723A (en) 2001-03-26
CA2314490A1 (en) 1999-06-24
DE69822513D1 (en) 2004-04-22
DK1047695T3 (en) 2004-06-28
HUP0102307A2 (en) 2001-12-28
SE9704709D0 (en) 1997-12-17
IS5522A (en) 2000-06-02
ATE261964T1 (en) 2004-04-15
DE69822513T2 (en) 2005-03-10
NO20003137D0 (en) 2000-06-16
NZ504909A (en) 2001-11-30
ES2216337T3 (en) 2004-10-16
CN1284956A (en) 2001-02-21
SK7812000A3 (en) 2001-05-10
EE200000365A (en) 2001-10-15
PL341388A1 (en) 2001-04-09
EP1047695B1 (en) 2004-03-17
BR9813668A (en) 2000-10-17
TR200001757T2 (en) 2000-09-21
IL136374A0 (en) 2001-06-14
NO20003137L (en) 2000-08-17
HUP0102307A3 (en) 2002-02-28
JP2002508375A (en) 2002-03-19
SI1047695T1 (en) 2004-08-31
EP1047695A1 (en) 2000-11-02
WO1999031100A1 (en) 1999-06-24
ID24638A (en) 2000-07-27
PT1047695E (en) 2004-07-30
US6291475B1 (en) 2001-09-18
ZA9811130B (en) 1999-06-17
AU1795399A (en) 1999-07-05

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